Christopher Michael Poteat

Works (4)

Updated: July 5th, 2023 15:29

2021 personal communication

Stereospecific Synthesis of Enantioenriched Alkylidenecyclobutanones via Formal Vinylidene Insertion into Cyclopropanone Equivalents

Poteat, C. M., & Lindsay, V. N. G. (2021, August 20).

By: C. Poteat n & V. Lindsay n 

TL;DR: 1-Sulfonylcyclopropanols are employed here as efficient cyclopropanone equivalents in a formal vinylidene insertion process, providing the first general synthetic route to enantioenriched alkylidenecyclobutanones after elimination. (via Semantic Scholar)
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Sources: Web Of Science, ORCID, NC State University Libraries
Added: August 10, 2021

2020 journal article

Enantioselective Synthesis of Cyclopropanone Equivalents and Application to the Formation of Chiral β-Lactams

Angewandte Chemie International Edition, 59(42), 18655–18661.

By: C. Poteat n, Y. Jang n, M. Jung n, J. Johnson  n, R. Williams n & V. Lindsay  n

author keywords: cycloaddition; lactams; ring expansion; small-ring compounds; synthetic methods
TL;DR: Both the electronic and steric nature of the sulfonyl moiety were found to have a crucial impact on the rate of equilibration to the corresponding cyclopropanone, highlighting their modular nature and the potential for their widespread adoption as synthetic intermediates. (via Semantic Scholar)
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Sources: Web Of Science, ORCID, NC State University Libraries
Added: September 7, 2020

2020 journal article

General Synthesis of Cyclopropanols via Organometallic Addition to 1-Sulfonylcyclopropanols as Cyclopropanone Precursors

Organic Letters, 22(16), 6510–6515.

By: R. Rivera  n, Y. Jang n, C. Poteat n & V. Lindsay n 

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Sources: Web Of Science, ORCID, NC State University Libraries, Crossref
Added: September 14, 2020

2019 journal article

Controlled -mono- and ,-di-halogenation of alkyl sulfones using reagent-solvent halogen bonding

CHEMICAL COMMUNICATIONS, 55(20), 2912–2915.

By: C. Poteat n & V. Lindsay n 

TL;DR: The direct and selective α-mono-bromination of alkyl sulfones was achieved through base-mediated electrophilic halogenation and the mono-halogenation was successfully extended to the fully selective β-chlorination, α-iodination and α-fluorination ofAlkyl sulphones. (via Semantic Scholar)
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Sources: Web Of Science, ORCID, NC State University Libraries
Added: April 15, 2019

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